Maropitant citrate exhibits rapid absorption, short half-life, and fast clearance in orange-winged Amazon parrots (Amazona amazonica) following subcutaneous and intravenous administration.

IF 1.3 3区 农林科学 Q2 VETERINARY SCIENCES
Ariella Darvish, David Sanchez-Migallon Guzman, Hugues Beaufrère, Heather K Knych, Olivia A Petritz
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引用次数: 0

Abstract

Objective: To determine pharmacokinetic parameters after IV and SC administration of a single dose of maropitant.

Methods: In this experimental study, adult orange-winged Amazon parrots were administered a single dose of maropitant (1 mg/kg) SC and IV with an 8-week washout period between experiments. Blood samples were collected at 0.5, 1.5, 2, 3, 6, 9, 12, and 24 hours after drug administration for the SC study. For the IV study, samples were taken at the same time points with additional collections at 5 minutes and 36 hours. Plasma maropitant was determined with LC-MS-MS, and pharmacokinetic parameters were calculated using a noncompartmental model.

Results: A total of 8 orange-winged Amazon parrots (2 female and 6 male) were used in this study. Mean ± SD maximum concentration after SC administration was 130.9 ± 24.6 ng/mL and was reached at 0.5 ± 0 hours. Combined terminal half-life after SC administration was 6.67 hours. Bioavailability after SC administration was 85%. Plasma concentration at 24 hours was negligible and nearly identical between SC and IV administrations.

Conclusions: A single dose of 1 mg/kg was well tolerated in all birds IV and SC. Maropitant rapidly attained plasma concentrations following SC administration and had a relatively high bioavailability and short half-life.

Clinical relevance: The results of this study suggest that the currently used doses and dosing intervals for maropitant in psittacine birds do not maintain above-target plasma concentrations considered therapeutic in dogs and may be insufficient to achieve systemic effects comparable to those observed in other species.

桔翼亚马逊鹦鹉皮下和静脉给药后,柠檬酸马匹坦吸收迅速,半衰期短,清除迅速。
目的:测定单剂量马洛匹坦静脉注射和皮下注射后的药动学参数。方法:在实验研究中,成年橙翅亚马逊鹦鹉被给予单剂量的马洛匹坦(1 mg/kg) SC和IV,两次实验之间有8周的洗脱期。在给药后0.5、1.5、2、3、6、9、12和24小时采集血样进行SC研究。对于静脉注射研究,在相同的时间点采集样本,并在5分钟和36小时额外采集。采用LC-MS-MS测定血浆马洛匹坦,采用非室室模型计算药代动力学参数。结果:本研究共使用8只亚马逊橙翅鹦鹉(雌性2只,雄性6只)。SC给药后的平均±SD最大浓度为130.9±24.6 ng/mL,在0.5±0小时达到。SC给药后的终末半衰期为6.67小时。SC给药后生物利用度为85%。24小时血浆浓度可以忽略不计,在静脉注射和皮下注射之间几乎相同。结论:单剂量1 mg/kg在所有IV和SC鸟类中耐受良好。在SC给药后,马络匹坦迅速达到血浆浓度,具有相对较高的生物利用度和较短的半衰期。临床相关性:本研究的结果表明,目前使用的马洛匹坦在鹦鹉身上的剂量和给药间隔不能维持在狗身上被认为具有治疗作用的高于目标的血浆浓度,可能不足以达到与在其他物种中观察到的全身效应。
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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
期刊介绍: The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.
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